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作 者:Yuqing Pan Huagen Chen Ruijing Ma Yongqin Wu Heyuan Lun Aixi Wang Kai He Jingran Yu Ping He
机构地区:[1]Department of Immunology and Microbiology,Shanghai Jiao Tong University,School of Medicine,Shanghai 200025,China [2]Shanghai Reinovax Biologics Co.,Ltd.,Pudong New District,Shanghai 201210,China
出 处:《One Health Advances》2024年第1期317-326,共10页全健康进展(英文)
基 金:funded by the the National Key Research and development Project of China(grant no.2022YFA1304300);National Natural Science Foundation of China(grant no.81971896).
摘 要:Carbapenem-resistant Klebsiella pneumoniae(CRKP)is emerging as an imminent threat to worldwide public health because of its high level of antimicrobial resistance,which can result in severe and challenging-to-treat infections.The capsular polysaccharide(CPS)of bacteria is well acknowledged as a crucial virulence factor that shields K.pneumoniae from the host’s innate immune system.Polysaccharide depolymerase,encoded by bacteriophages,can hydrolyze the CPS of K.pneumoniae and may be a promising approach for treating K.pneumoniae infections.In this study,we identified a novel K62-type capsule depolymerase(K62-Dpo30)from the K.pneumoniae phage SH-KP2492.We dem-onstrated that the K62-Dpo30 depolymerase could specifically degrade the CPS of K62-type K.pneumoniae strains and promote the susceptibility of K62-type K.pneumoniae strains to serum and neutrophil killing.Furthermore,our findings highlight the potential of the K62-Dpo30 depolymerase as a reliable K.pneumoniae capsular typing tool.
关 键 词:Klebsiella pneumoniae BACTERIOPHAGE Capsule depolymerase
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